Evidence map›Paper›PMID 35209126›Full record

ArticleMolecules (Basel, Switzerland)2022

Synthesis and Structure-Activity Relationship Studies of Benzimidazole-4,7-dione-Based P2X3 Receptor Antagonists as Novel Anti-Nociceptive Agents.

Jinsu Bae, Yeo-Ok Kim, Xuehao Han, Myung-Ha Yoon, Woong-Mo Kim, Yong-Chul Kim

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.2field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Jinsu BaeDepartment of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.
Yeo-Ok KimDepartment of Anesthesiology and Pain Medicine, Chonnam National University Medical School, Gwangju 61469, Korea.
Xuehao HanDepartment of Anesthesiology and Pain Medicine, Chonnam National University Medical School, Gwangju 61469, Korea.
Myung-Ha YoonDepartment of Anesthesiology and Pain Medicine, Chonnam National University Medical School, Gwangju 61469, Korea.
Woong-Mo KimDepartment of Anesthesiology and Pain Medicine, Chonnam National University Medical School, Gwangju 61469, Korea.
Yong-Chul KimDepartment of Biomedical Science and Engineering, Gwangju Institute of Science and Technology (GIST), Gwangju 61005, Korea.
Gwangju Institute of Science and Technology · KRChonnam National University Hospital · KR

Funding

Chonnam National University Hospital BCRI20049Gwangju Institute of Science and Technology 2020
6 · The paper itself

Abstract

P2X3 receptors (P2X3R) are ATP-gated ion channels predominantly expressed in C- and Aδ-fiber primary afferent neurons and have been introduced as a novel therapeutic target for neurological disorders, including neuropathic pain and chronic cough. Because of its localized distribution, antagonism of P2X3R has been thoroughly considered, and the avoidance of issues related to CNS side effects has been proven in clinical trials. In this article, benzimidazole-4,7-dione-based derivatives were introduced as a new chemical entity for the development of P2X3R antagonists. Starting from the discovery of a hit compound from the screening of 8364 random library compounds in the Korea Chemical Bank, which had an IC

Indexed as

AnalgesicsAnimalsBenzimidazolesChemistry Techniques, SyntheticDisease Models, AnimalDose-Response Relationship, DrugDrug Evaluation, PreclinicalDrug MonitoringHumansMiceMolecular StructurePurinergic P2X Receptor AntagonistsRatsSmall Molecule LibrariesStructure-Activity RelationshipAnalgesicsBenzimidazolesPurinergic P2X Receptor AntagonistsSmall Molecule Librariesadenosine 5′-triphosphateantagonistanti-nociceptive agentsneuropathic painP2X3 receptorstructure−activity relationship study

Identifiers

PMID35209126
PMCPMC8877008
OpenAlexW4212794289

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.